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PharmaCompass offers a list of Noscapine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Noscapine manufacturer or Noscapine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Noscapine manufacturer or Noscapine supplier.
PharmaCompass also assists you with knowing the Noscapine API Price utilized in the formulation of products. Noscapine API Price is not always fixed or binding as the Noscapine Price is obtained through a variety of data sources. The Noscapine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Boots Brand of Noscapine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Boots Brand of Noscapine Hydrochloride, including repackagers and relabelers. The FDA regulates Boots Brand of Noscapine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Boots Brand of Noscapine Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Boots Brand of Noscapine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Boots Brand of Noscapine Hydrochloride supplier is an individual or a company that provides Boots Brand of Noscapine Hydrochloride active pharmaceutical ingredient (API) or Boots Brand of Noscapine Hydrochloride finished formulations upon request. The Boots Brand of Noscapine Hydrochloride suppliers may include Boots Brand of Noscapine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Boots Brand of Noscapine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Boots Brand of Noscapine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Boots Brand of Noscapine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Boots Brand of Noscapine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Boots Brand of Noscapine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Boots Brand of Noscapine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Boots Brand of Noscapine Hydrochloride USDMF includes data on Boots Brand of Noscapine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Boots Brand of Noscapine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Boots Brand of Noscapine Hydrochloride suppliers with USDMF on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Boots Brand of Noscapine Hydrochloride Drug Master File in Japan (Boots Brand of Noscapine Hydrochloride JDMF) empowers Boots Brand of Noscapine Hydrochloride API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Boots Brand of Noscapine Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Boots Brand of Noscapine Hydrochloride JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Boots Brand of Noscapine Hydrochloride suppliers with JDMF on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Boots Brand of Noscapine Hydrochloride Drug Master File in Korea (Boots Brand of Noscapine Hydrochloride KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Boots Brand of Noscapine Hydrochloride. The MFDS reviews the Boots Brand of Noscapine Hydrochloride KDMF as part of the drug registration process and uses the information provided in the Boots Brand of Noscapine Hydrochloride KDMF to evaluate the safety and efficacy of the drug.
After submitting a Boots Brand of Noscapine Hydrochloride KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Boots Brand of Noscapine Hydrochloride API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Boots Brand of Noscapine Hydrochloride suppliers with KDMF on PharmaCompass.
A Boots Brand of Noscapine Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Boots Brand of Noscapine Hydrochloride Certificate of Suitability (COS). The purpose of a Boots Brand of Noscapine Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Boots Brand of Noscapine Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Boots Brand of Noscapine Hydrochloride to their clients by showing that a Boots Brand of Noscapine Hydrochloride CEP has been issued for it. The manufacturer submits a Boots Brand of Noscapine Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Boots Brand of Noscapine Hydrochloride CEP holder for the record. Additionally, the data presented in the Boots Brand of Noscapine Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Boots Brand of Noscapine Hydrochloride DMF.
A Boots Brand of Noscapine Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Boots Brand of Noscapine Hydrochloride CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Boots Brand of Noscapine Hydrochloride suppliers with CEP (COS) on PharmaCompass.
A Boots Brand of Noscapine Hydrochloride written confirmation (Boots Brand of Noscapine Hydrochloride WC) is an official document issued by a regulatory agency to a Boots Brand of Noscapine Hydrochloride manufacturer, verifying that the manufacturing facility of a Boots Brand of Noscapine Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Boots Brand of Noscapine Hydrochloride APIs or Boots Brand of Noscapine Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Boots Brand of Noscapine Hydrochloride WC (written confirmation) as part of the regulatory process.
click here to find a list of Boots Brand of Noscapine Hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Boots Brand of Noscapine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Boots Brand of Noscapine Hydrochloride API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Boots Brand of Noscapine Hydrochloride as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Boots Brand of Noscapine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Boots Brand of Noscapine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Boots Brand of Noscapine Hydrochloride suppliers with NDC on PharmaCompass.
Boots Brand of Noscapine Hydrochloride Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.
GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).
PharmaCompass offers a list of Boots Brand of Noscapine Hydrochloride GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Boots Brand of Noscapine Hydrochloride GMP manufacturer or Boots Brand of Noscapine Hydrochloride GMP API supplier for your needs.
A Boots Brand of Noscapine Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Boots Brand of Noscapine Hydrochloride's compliance with Boots Brand of Noscapine Hydrochloride specifications and serves as a tool for batch-level quality control.
Boots Brand of Noscapine Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Boots Brand of Noscapine Hydrochloride CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.
Boots Brand of Noscapine Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Boots Brand of Noscapine Hydrochloride EP), Boots Brand of Noscapine Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Boots Brand of Noscapine Hydrochloride USP).
